# FDA Inspection 1099709 - Nordmark Arzneimittel GMBH & Co. KG - August 16, 2019

Source: https://www.keypedia.com/records/fda_inspections/nordmark-arzneimittel-gmbh-co-kg/65cc61b2-c4a2-4b16-8979-09c66710a18d
Source feed: FDA_Inspections

> FDA Inspection 1099709 for Nordmark Arzneimittel GMBH & Co. KG on August 16, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099709
- Company Name: Nordmark Arzneimittel GMBH & Co. KG
- Inspection Date: 2019-08-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Company: https://www.keypedia.com/companies/nordmark-arzneimittel-gmbh-co-kg/871eb270-8517-4646-923a-b4d2eb0ea73b

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
